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HRID 218323作成日:2026年10月24日

N'-Hydroxybenzenecarboximidamide → 4-Benzyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)morpholine

https://huagongshe.com/ja/reaction/218323

反応式

関与物質

役割名称HCID仕込み量
反応物N'-HydroxybenzenecarboximidamideHCID 69186—
反応物DiisopropylethylamineHCID 81531—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物4-Benzylmorpholine-2-carboxylic acid hydrochlorideHCID 2776352—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-Benzyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)morpholineHCID 4695671177%

反応手順

To a stirred solution of 4-benzyl-2-morpholinecarboxylic acid hydrochloride (intermediate 20, 1.5 g, 5.82 mmol) in N,N-dimethylformamide (10 ml) was added 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluroniumtetrafluoroborate (2.2 g, 6.98 mmol), 1-hydroxybenzotriazole hydrate (236 mg, 1.74 mmol) and N,N-diisopropylethylamine (5.1 ml, 29.1 mmol), and the reaction mixture was stirred at room temperature for 30 minutes. After the addition of N′-hydroxybenzamidine (792 mg, 5.82 mmol), the reaction mixture was stirred at room temperature for one hour, and then heated to 110° C. When the reaction was complete (checked by thin layer chromatography), excess reagent was decomposed by the addition of water and the aqueous layer was extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate, and concentrated in vacuo. The resulting residue was purified by column chromatography on silica gel, (eluent; 25% ethyl acetate in hexane) to afford 4-benzyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)morpholine (intermediate 21, 1.44 g, 77%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198437B2
出典データセットuspto-grants-2012_06
ORD IDord-7841db3106c34e3c9282b61dd83d6901
出典メモuspto-grants-2012_06